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471348

Sigma-Aldrich

Methanesulfonic acid solution

70 wt. % in H2O

Synonym(s):

Mesylic acid, MsOH

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About This Item

Linear Formula:
CH3SO3H
CAS Number:
Molecular Weight:
96.11
Beilstein:
1446024
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

vapor density

3.3 (vs air)

Quality Level

vapor pressure

<1 mmHg ( 20 °C)

concentration

70 wt. % in H2O

impurities

≤1,000 ppm Sulfate (SO4)
≤10 ppm Iron
≤50 ppm Chloride (Cl)

refractive index

n20/D 1.416

density

1.319 g/mL at 25 °C

functional group

sulfonic acid

SMILES string

CS(O)(=O)=O

InChI

1S/CH4O3S/c1-5(2,3)4/h1H3,(H,2,3,4)

InChI key

AFVFQIVMOAPDHO-UHFFFAOYSA-N

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General description

The product is a 70% aqueous solution of methanesulfonic acid (MSA). MSA is a strong organic acid. The chemical oxidation of dimetyl sulfide in the atmosphere leads to the formation of MSA in large quantities. MSA undergoes biodegradation by forming CO2 and sulphate. It is considered a green acid as it is less toxic and corrosive in comparison to mineral acids.1 The aqueous MSA solution has been considered a model electrolyte for electrochemical processes.

Application

Methanesulfonic acid solution may be used to study the corrosion behavior of stainless steel.

Legal Information

Product of Arkema Inc.

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Customers Also Viewed

Corrosion behaviour of stainless steels in aqueous solutions of methanesulfonic acid.
Finsgar M and Milosev I.
Corrosion Science, 52(7), 2430-2438 (2010)
Microbial metabolism of methanesulfonic acid.
Kelly DP and Murrell JC.
Archives of Microbiology, 172(6), 341-348 (1999)
Methane Sulphonic Acid is Green Catalyst in Organic Synthesis.
Kulkarni P.
Orient. J. Chem., 31(1), 447-451 (2015)
Environmental benefits of methanesulfonic acid. Comparative properties and advantages.
Gernon MD.
Green Chemistry, 1(3), 127-140 (1999)
Eric D Nacsa et al.
Organic letters, 15(1), 38-41 (2012-12-15)
The cyclopropenone catalyzed nucleophilic substitution of alcohols by methanesulfonate ion with inversion of configuration is described. This work provides an alternative to the Mitsunobu reaction that avoids the use of azodicarboxylates and generation of hydrazine and phosphine oxide byproducts. This

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